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      Colloidal Synthesis and Characterization of Molybdenum Chalcogenide Quantum Dots Using a Two-Source Precursor Pathway for Photovoltaic Applications

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          Abstract

          The drawbacks of utilizing nonrenewable energy have quickened innovative work on practical sustainable power sources (photovoltaics) because of their provision of a better-preserved decent environment which is free from natural contamination and commotion. Herein, the synthesis, characterization, and application of Mo chalcogenide nanoparticles (NP) as alternative sources in the absorber layer of QDSSCs is discussed. The successful synthesis of the NP was confirmed as the results from the diffractive peaks obtained from XRD which were positive and agreed in comparison with the standard. The diffractive peaks were shown in the planes (100), (002), (100), and (105) for the MoS 2 nanoparticles; (002), (100), (103), and (110) for the MoSe 2 nanoparticles; and (0002), (0004), (103), as well as (0006) for the MoTe 2 nanoparticles. MoSe 2 presented the smallest size of the nanoparticles, followed by MoTe 2 and, lastly, by MoS 2. These results agreed with the results obtained using SEM analysis. For the optical properties of the nanoparticles, UV–Vis and PL were used. The shift of the peaks from the red shift (600 nm) to the blue shift (270–275 nm and 287–289 nm (UV–Vis)) confirmed that the nanoparticles were quantum-confined. The application of the MoX 2 NPs in QDSSCs was performed, with MoSe 2 presenting the greatest PCE of 7.86%, followed by MoTe 2 (6.93%) and, lastly, by MoS 2, with the PCE of 6.05%.

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          Solar energy conversion by dye-sensitized photovoltaic cells.

          The quality of human life depends to a large degree on the availability of energy. This is threatened unless renewable energy resources can be developed in the near future. Chemistry is expected to make important contributions to identify environmentally friendly solutions of the energy problem. One attractive strategy discussed in this Forum Article is the development of solar cells that are based on the sensitization of mesoscopic oxide films by dyes or quantum dots. These systems have already reached conversion efficiencies exceeding 11%. The underlying fundamental processes of light harvesting by the sensitizer, heterogeneous electron transfer from the electronically excited chromophore into the conduction band of the semiconductor oxide, and percolative migration of the injected electrons through the mesoporous film to the collector electrode will be described below in detail. A number of research topics will also be discussed, and the examples for the first outdoor application of such solar cells will be provided.
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            Transition metal dichalcogenides and beyond: synthesis, properties, and applications of single- and few-layer nanosheets.

            CONSPECTUS: In the wake of the discovery of the remarkable electronic and physical properties of graphene, a vibrant research area on two-dimensional (2D) layered materials has emerged during the past decade. Transition metal dichalcogenides (TMDs) represent an alternative group of 2D layered materials that differ from the semimetallic character of graphene. They exhibit diverse properties that depend on their composition and can be semiconductors (e.g., MoS2, WS2), semimetals (e.g., WTe2, TiSe2), true metals (e.g., NbS2, VSe2), and superconductors (e.g., NbSe2, TaS2). The properties of TMDs can also be tailored according to the crystalline structure and the number and stacking sequence of layers in their crystals and thin films. For example, 2H-MoS2 is semiconducting, whereas 1T-MoS2 is metallic. Bulk 2H-MoS2 possesses an indirect band gap, but when 2H-MoS2 is exfoliated into monolayers, it exhibits direct electronic and optical band gaps, which leads to enhanced photoluminescence. Therefore, it is important to learn to control the growth of 2D TMD structures in order to exploit their properties in energy conversion and storage, catalysis, sensing, memory devices, and other applications. In this Account, we first introduce the history and structural basics of TMDs. We then briefly introduce the Raman fingerprints of TMDs of different layer numbers. Then, we summarize our progress on the controlled synthesis of 2D layered materials using wet chemical approaches, chemical exfoliation, and chemical vapor deposition (CVD). It is now possible to control the number of layers when synthesizing these materials, and novel van der Waals heterostructures (e.g., MoS2/graphene, WSe2/graphene, hBN/graphene) have recently been successfully assembled. Finally, the unique optical, electrical, photovoltaic, and catalytic properties of few-layered TMDs are summarized and discussed. In particular, their enhanced photoluminescence (PL), photosensing, photovoltaic conversion, and hydrogen evolution reaction (HER) catalysis are discussed in detail. Finally, challenges along each direction are described. For instance, how to grow perfect single crystalline monolayer TMDs without the presence of grain boundaries and dislocations is still an open question. Moreover, the morphology and crystal structure control of few-layered TMDs still requires further research. For wet chemical approaches and chemical exfoliation methods, it is still a significant challenge to control the lateral growth of TMDs without expansion in the c-axis direction. In fact, there is plenty of room in the 2D world beyond graphene. We envisage that with increasing progress in the controlled synthesis of these systems the unusual properties of mono- and few-layered TMDs and TMD heterostructures will be unveiled.
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              Universal Approach toward Hysteresis-Free Perovskite Solar Cell via Defect Engineering

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                Author and article information

                Contributors
                Role: Academic Editor
                Journal
                Molecules
                Molecules
                molecules
                Molecules
                MDPI
                1420-3049
                09 July 2021
                July 2021
                : 26
                : 14
                : 4191
                Affiliations
                [1 ]Fort Hare Institute of Technology (FHIT), Private Bag X1314, Alice 5700, South Africa; 201515550@ 123456ufh.ac.za (E.C.); emeyer@ 123456ufh.ac.za (E.M.)
                [2 ]Department of Chemistry, University of Fort Hare, Alice 5700, South Africa; jmbese@ 123456ufh.ac.za
                [3 ]Energy, Materials and Inorganic Chemistry Research Group (EMICREG), University of Fort Hare, Alice 5700, South Africa
                Author notes
                [* ]Correspondence: nzingwe@ 123456ufh.ac.za ; Tel.: +27-62-340-6507
                Author information
                https://orcid.org/0000-0002-9377-7083
                https://orcid.org/0000-0002-9912-311X
                https://orcid.org/0000-0001-9136-9302
                https://orcid.org/0000-0002-3775-9016
                Article
                molecules-26-04191
                10.3390/molecules26144191
                8307795
                34299466
                14974151-0725-469b-828f-82d1fd5459c3
                © 2021 by the authors.

                Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license ( https://creativecommons.org/licenses/by/4.0/).

                History
                : 11 April 2021
                : 06 July 2021
                Categories
                Article

                chalcogenides,metals,chemical synthesis
                chalcogenides, metals, chemical synthesis

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